The following data is part of a premarket notification filed by Safe Orthopaedics with the FDA for Sterispine Lc Cage.
Device ID | K133893 |
510k Number | K133893 |
Device Name: | STERISPINE LC CAGE |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | SAFE ORTHOPAEDICS Parc Des Bellevues Allee R.Luxembourg-Bat Californie Eragny Sur Oise, FR 95610 |
Contact | Pierre Dumouchel |
Correspondent | Pierre Dumouchel SAFE ORTHOPAEDICS Parc Des Bellevues Allee R.Luxembourg-Bat Californie Eragny Sur Oise, FR 95610 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-12-20 |
Decision Date | 2014-03-14 |
Summary: | summary |